R. Lowen

Benign substitution (Aα289 Arg→Gln) in the αC region of human fibrinogen.

Ryan L. Davis, S. Brennan, R. Lowen, 2010, Blood cells, molecules & diseases.

Deletion of five residues from the coiled coil of fibrinogen (Bβ Asn167_Glu171del) associated with bleeding and hypodysfibrinogenemia

Ryan L. Davis, S. Brennan, R. Lowen, 2009, Haematologica.

Hypofibrinogenaemia resulting from novel single nucleotide deletion at codon Bβ58 (3404del A) associated with thrombotic stroke in infancyHypofibrinogenaemia resulting from novel single nucleotide deletion at codon

S. Brennan, K. Siebenlist, M. Mosesson, 2006 .

Aeromonas hydrophila infection complicating digital replantation and revascularization.

D. Phelps, R. Lowen, L. Ketch, 1989, The Journal of hand surgery.

Congenital hypodysfibrinogenaemia (Fibrinogen Des Moines) due to a γ320Asp deletion at the Ca2+ binding site

S. Brennan, M. Mosesson, R. Lowen, 2007, Thrombosis and Haemostasis.

Hypofibrinogenaemia resulting from novel single nucleotide deletion at codonbrBbeta;58 (3404del A) associated with thrombotic stroke in infancyHypofibrinogenaemia resulting from novel single nucleotide deletion at codon

S. Brennan, M. Mosesson, R. Lowen, 2017 .

Dysfibrinogenemia (fibrinogen Wilmington) due to a novel Aα chain truncation causing decreased plasma expression and impaired fibrin polymerisation

S. Brennan, M. Mosesson, C. Frantz, 2006, Thrombosis and Haemostasis.

Hypofibrinogenaemia resulting from novel single nucleotide deletion at codon Bβ58 (3404del A) associated with thrombotic stroke in infancy

S. Brennan, M. Mosesson, R. Lowen, 2006, Thrombosis and Haemostasis.